Sofia De Anchorena Email & Phone Number

I worked as a Clinical Trial Coordinator for 1 year and 1 month, my experience is Management of all regulatory documentation of the study. (opening, development and closing of the same).Maintenance and updating of Research Files.Uploading of imaging studies and laboratories to the corresponding platforms.Equipment calibration.Management of different database entry systems (electronic CRF)Medical assistance and assistance to the research subject during the development of the study.Reception, storage and dispensing of study drugs according to the applicable system (IVRS, IWRS, Clinphone, among others).Preparation and sending of progress/final reports to the corresponding health entities and Ethics Committees.Experience in ANMAT inspections and Independent Ethics Committee Audits.Review, update and compliance with Standard Operating Procedures (SOPs).